<div class="application article clearfix" id="description">
<p class="printTableText" lang="en">New Zealand Paient Spedficaiion for Paient Number 537253 <br><br>
WO 03/097058 PCT/EP03/05226 <br><br>
NEW PHARMACEXJTICAL COMPOSITIONS CONTAINING FLIBANSERIN POLYMORPH A <br><br>
The invention relates to oral pharmaceutical compositions containing flibanserin, methods for the preparation thereof and use thereof as a medicament. <br><br>
10 <br><br>
Background of the invention The compound 1 -[2-(4-(3-trifluoromethyl-phenyl)piperazin-1 -yl)ethyl]-2,3-dihydro-1 H-benzimidazol-2-one (flibanserin) is disclosed in form of its hydrochlorid in European Patent Application EP-A-526434 and has the following chemical structure: <br><br>
.CFo <br><br>
OO <br><br>
1 xHCI <br><br>
Flibanserin shows affinity for the 5-HTia and 5-HT2-receptor. It is therefore a promising therapeutic agent for the treatment of a variety of diseases, for instance 15 depression, schizophrenia, Parkinson, anxiety, sleep disturbances, sexual and mental disorders and age associated memory impairment. <br><br>
A certain pharmaceutical activity is of course the basic prerequisite to be fulfilled by a pharmaceutically active agent before same is approved as a medicament on the 20 market. However, there are a variety of additional requirements a pharmaceutically ' active agent has to comply with. These requirements are based on various parameters which are connected with the nature of the active substance itself. Without being restrictive, examples of these parameters are the stability of the active agent under various environmental conditions, its stability during production of the 25 pharmaceutical formulation and the stability of the active agent in the final medicament compositions. The pharmaceutically active substance used for preparing the pharmaceutical compositions should be as pure as possible and its stability in long-term storage must be guaranteed under various environmental conditions. This is absolutely essential to prevent the use of pharmaceutical 30 compositions which contain, in addition to the actual active substance, degradation products thereof, for example. In such cases the content of active substance in the medicament might be less than that specified. <br><br>
Uniform distribution of the active substance in the formulation is a critical factor, 35 particularly when the medicament has to be given in low doses. To ensure uniform <br><br>
2 <br><br>
distribution, the particle size of the active substance can be reduced to a suitable level, e.g. by grinding. Since degradation and/or amorphization of the pharmaceutically active substance as a side effect of the grinding (or micronising) has to be avoided as far as possible, in spite of the hard conditions required during the process, it is absolutely essential 5 that the active substance should be highly stable throughout the grinding process. Only if the active substance is sufficiently stable during the grinding process is it possible to produce a homogeneous pharmaceutical formulation which always contains the specified amount of active substance in reproducible manner. <br><br>
10 Finally, the properties of the pharmaceutical composition as such decisively contribute to the bioavailability of the active agent and hence efficacy of the medicament in the intended medical use. <br><br>
The aim of the invention is thus to provide a new formulation for oral administration 15 containing flibanserin which meets the stringent requirements imposed on pharmaceutical compositions as mentioned above. This aim should be read disjunctively with the further aim of at least providing a useful alternative to known formulations. <br><br>
Description of the invention 20 It has been found, surprisingly, that the free base of flibanserin in a specific polymophic form best fulfils the requirements to be met within the formulation according to the invention. This specific polymorphic form (polymorph A) is obtainable by specific reaction conditions which are described in more detail hereinbelow. Among other features this polymorphic form is characterized by an endothermic maximum at 161°C which occurs during thermal analysis 25 using DSC (Differential Scanning Calorimetry). <br><br>
The pharmaceutical composition according to the invention is a tablet for oral administration comprising a core, containing flibanserin polymorph A being characterized by an endothermic maximum at 161°C determined by DSC in admixture with at least one 30 pharmaceutically acceptable excipient and further comprising a film coating enveloping said core. <br><br>
Based on the total mass of the core of the film-coated tablets according to the invention flibanserin polymorph A is present in amounts of 1 to 50 wt.%, preferably 5 to 45 wt.%, 35 particularly preferably about 10 to 40 wt.%. Particularly preferably, the proportion of flibanserin polymorph A is between 15 and 35 wt.%, more preferably between 17 and 32 wt.% based on the total mass of the core. <br><br>
intellectual property office of n.z. <br><br>
1 <i JUN 2007 <br><br>
RECEIVED <br><br>
WO 03/097058 <br><br>
PCT/EP03/05226 <br><br>
3 <br><br>
The core of the pharmaceutical formulation according to the invention contains, in addition to flibanserin polymorph A, at least one excipient as filler/dry binder. <br><br>
Within the scope of the present invention typical fillers are for example lactose monohydrate, both fine milled material or modified lactose like spray-dried lactose 5 and agglomerated lactose (Tablettose), anhydrous lactose,microcrystalline cellulose, dibasic calcium phosphate, cornstarch, sugar alcohols like e.g. mannitol and sorbitol and mixtures thereof. Preferably the filler within the formulation according to the invention is selected from the group consisting of lactose types, microcrystalline cellulose, cornstarch, sugar alcohols and mixtures thereof. More preferably the filler 10 in the formulation according to the invention is selected from the group consisting of lactose types, microcrystalline cellulose, and mixtures thereof. If lactose is used as a filler it is preferably applied in form of the lactose monohydrate fine milled material (e.g. 200 mesh grade). <br><br>
15 The core of the film-coated tablet according to the invention may also contain dry and/or wet binding agents, such as povidone (e.g. Kollidon K 25), copovidone (e.g. Kollidon VA 64), hydroxypropyl methylcellulose, hydroxypropylcellulose, corn starch and mixtures thereof. Preferably the binding agent is selected from the group of povidone, hydroxypropyl methylcellulose, hydroxypropyl ethylcellulose, 20 hydroxypropylcellulose, and mixtures thereof. Most preferably hydroxyproypl methylcellulose is selected as.binding agent. If hydroxypropyl methylcellulose (HPMC) is applied the HPMC polymers HPMC USP2910 and USP2208 like for instance Methocel E5, E4M, E15M, (K15M, and K100M) supplied for instance by the Dow Chemical Company are of special interest. In the aforementioned abbreviations the designation "E" refers to USP2910 whereas "K" refers to USP2208. The number designation refers to the viscosity in a 2% aqueous solution (e.g. 5 designates a viscosity of 5 cps; 15M designates a viscosity of 15000 cps). <br><br>
Based on the total mass of the core of the film-coated tablets according to the 30 invention the filler is preferably present in amounts of 50 to 99 wt.%, preferably 55 to 95 wt.%, particularly preferably about 60 to 90 wt.%. Particularly preferably, the proportion of the total amount of filler is between 65 and 85 wt.%, more preferably . between 68 and 80 wt.% based on the total mass of the core. <br><br>
35 Preferably the core of the tablet formulation according to the invention comprises flibanserin polymorph A in admixture with lactose monohydrate as the pharmaceutically acceptable excipient. <br><br>
More preferably the core of the tablet formulation according to the invention comprises flibanserin polymorph A in admixture with lactose monohydrate and <br><br>
WO 03/097058 <br><br>
PCT/EP03/05226 <br><br>
4 <br><br>
microcrystalline cellulose as pharmaceutically acceptable excipients. In formulations according to the invention containing a mixture of lactose monohydrate and microcrystalline cellulose as filler components (or pharmaceutically acceptable excipients), the ratio of lactose monohydrate to microcrystalline cellulose is for 5 example in the range of about 15:1 to about 1:5, preferably in a range of about 10:1 to about 1:3, more preferably in a range of about 6:1 to about 1:1. <br><br>
In another preferred embodiment according to the invention tablet formulation comprises flibanserin polymorph A in admixture with lactose monohydrate, 10 microcrystalline cellulose and HPMC as pharmaceutically acceptable excipients. In particular preferred formulations according to the invention containing a mixture of lactose monohydrate, microcrystalline cellulose and HPMC as filler/binder components (or pharmaceutically acceptable excipients), the amount of lactose monohydrate is for example in the range of 50 to 95 wt.%, preferably 60 to 90 wt.%, 15 more preferably about 65 to 85 wt.% based on the total mass of the filler/binder used for the preparation of the core. In a particularly preferred embodiment these tablet formulations contain lactose monohydrate in an amount of about 70 to 80 wt.% based on the total mass of the filler/binder used for the preparation of the core. In the particular preferred formulations according to the invention containing a mixture of 20 lactose monohydrate, microcrystalline cellulose and HPMC as filler/binder components (or pharmaceutically acceptable excipients), the amount of microcrystalline cellulose is for example in the range of 5 to 45 wt.%, preferably 15 to 35 wt.%, more preferably about 20 to 30 wt.% based on the total mass of the filler/binder used for the preparation of the core. In a particularly preferred 025 embodiment these tablet formulations contain microcrystalline cellulose in an amount of about 22 to 28 wt.% based on the total mass of the filler/binder used for the preparation of the core. In the particularly preferred formulations according to the invention containing a mixture of lactose monohydrate, microcrystalline cellulose and HPMC as filler/binder components (or pharmaceutically acceptable excipients), the 30 amount of HPMC is for example in the range of 0.5 to 5 wt.%, preferably 1.0 to 4.5 wt.% based on the total mass of the filler/binder used for the preparation of the core. In a particularly preferred embodiment these tablet formulations contain HPMC in an amount of about 1 to 3 wt.% based on the total mass of the filler/binder used for the preparation of the core. <br><br>
35 <br><br>
The core of the film-coated tablet according to the invention may also contain disintegrants in addition to the ingredients mentioned above. Within the scope of the present invention these disintegrants may optionally also be known as breakdown agents. These are preferably selected according to the invention from among sodium <br><br>
WO 03/097058 <br><br>
PCT/EP03/05226 <br><br>
5 <br><br>
starch glycolate, crospovidone, croscarmellose sodium, sodium-carboxymethylceiiulose, dried corn starch and mixtures thereof. Particularly preferably, within the scope of the present invention, sodium starch glycolate, crospovidone, sodium-carboxymethylcellulose and croscarmellose sodium, 5 preferably croscarmellose sodium are used. If the abovementioned disintegrants are used, the amount by weight used based on the total mass of the core of the film-coated tablet according to the invention is for example in a range from about 0.1 -10 wt.%, preferably about 0.5 - 5 wt.%, more preferably about 1 - 3 wt.%. <br><br>
10 The core of the film-coated tablet according to the invention may also contain flow regulators as additional ingredients. Flow regulators within the scope of the present invention include, for example, silicon dioxide, talc, magnesium stearate and mixtures thereof. According to the invention silicon dioxide is preferably used, particularly preferably in colloidal, highly dispersed form.lf the abovementioned flow 15 regulators are used, the amount by weight thereof based on the total mass of the core of the film-coated tablet according to the invention is preferably in a range from about 0.1-5 wt.%, preferably about 0.3 - 2 wt.%, particularly preferably between 0.4 and 1.5 wt.%. <br><br>
20 The core of the film-coated tablet according to the invention may also contain flow agents, lubricants and mould release or antiadhesive agents as further ingredients. These include, for example, within the scope of the present invention, stearic acid, magnesium stearate, calcium stearate, sodium stearyl fumarate, glycerol tribehenate, talc and mixtures thereof. According to the invention, stearic acid and (^^5 magnesium stearate are preferably used. If one or several of the aforementioned ingredients is used the amount by weight thereof is preferably in a range from about 0.01 - 5 wt.%, preferably about 0.05 - 3 wt.%, particularly preferably about 0.1-2 wt.% based on the total mass of the core of the film-coated tablet. Preferably, especially in case of magnesium stearate the amount thereof is in the range of about 30 0.2 -1.5 wt.% based on the total mass of the core of the film-coated tablet. <br><br>
The film coating enveloping the core of the film-coated tablets according to the invention contains at least one or more film-forming agents selected from among hydroxypropylmethylcellulose, hydroxypropylcellulose, methylcellulose, 35 hydroxymethylcellulose, hydroxyethylcellulose and poly(ethylacryiate) <br><br>
methylmethacrylate, the latter in the form of Eudragit NE 30 D, for example. . Alternatively, Eudragit RL 30 D or Eudragit E 12.5 may be used, for example. The above ingredients may optionally also be used in the form of mixtures thereof. Preferred film-forming agents are hydroxypropylmethylcellulose, <br><br>
WO 03/097058 <br><br>
PCT/EP03/05226 <br><br>
6 <br><br>
hydroxypropylcellulose, hydroxymethylcellulose and hydroxyethylcellulose, of which hydroxypropylmethylcellulose and hydroxypropylcellulose are particularly preferred as film-forming agents according to the invention. The abovementioned film-forming agents may be used on their own or in the form of the mixtures thereof. If only one of the abovementioned film-forming agents is used, hydroxypropylmethylcellulose is of particular importance in this context within the scope of the present invention. The amount by weight of film-forming agents based on the total mass of the film coating of the film-coated tablet according to the invention is preferably in a range from about 20 - 95 wt.%, preferably 30 - 90 wt.% . <br><br>
10 <br><br>
The film coating enveloping the core may contain emulsifiers and/or plasticisers such as, for example, polyethyleneglycol, glycerol and propyleneglycol, optionally in the form of the mixtures thereof. Preferably, polyethyleneglycols are used as plasticisers. Without restricting the subject matter of the invention thereto, polyethyleneglycol 400 15 and polyethyleneglycol 6000 are examples of particularly preferred polyethyleneglycols. Within the description of the instant invention references to the term Macrogol are to be understood as references to the term polyethyleneglycol. The values 400 and 6000 mentioned hereinbefore indicate the average molecular weight of the polyethyleneglycol applied. The amount of plasticiser by weight based 20 on the total mass of the film coating of the film-coated tablet according to the invention is preferably in a range from about 1 - 50 wt.%, preferably 5-40 wt.%, particularly preferably 10-30 wt.%. Preferably the amount of plasticiser is in a range of about 10-25 wt.%, more preferably in a range of about 12 -18 wt.% based on the total mass of the film coating of the film-coated tablet. <br><br>
\25 <br><br>
The film coating of the film-coated tablet according to the invention may also contain coloured pigments and pigmenting excipients. Iron oxide, titanium dioxide, talc and mixtures thereof may be mentioned by way of example. In case talc is used the amount thereof is for example in a range from about 5 - 50 wt.%, preferably 10-40 30 wt.%, particularly preferably 15-30 wt.% based on the total mass of the film coating of the film-coated tablet. Preferably the amount of talc is in a range of about 15-20 wt.% based on the total mass of the film coating of the film-coated tablet, in case titanium dioxide is used the amount thereof is for example in a range from about 5 -55 wt.%, preferably 10-40 wt.%, particularly preferably 15-35 wt.% based on the 35 total mass of the film coating of the film-coated tablet. Preferably the amount of titanium dioxide is in a range of about 20 - 30 wt.% based on the total mass of the film coating of the film-coated tablet. In case iron oxide is used the amount thereof is for example in a range from about 0.1-5 wt.%, preferably about 0.25 - 3 wt.%, more <br><br>
WO 03/097058 <br><br>
preferably about 0.5 -film-coated tablet. <br><br>
PCT/EP03/05226 <br><br>
7 <br><br>
1.5 wt.% based on the total mass of the film coating of the <br><br>
In a particular preferred embodiment the film coat enveloping the core of the tablet 5 according to the invention comprises hydroxypropyl methylcellulose, <br><br>
polyethyleneglycol and titanium dioxide. In another embodiment according to the invention the film coat enveloping the core of the tablet according to the invention comprises hydroxypropyl methylcellulose, polyethyleneglycol, titanium dioxide and talc. In yet another embodiment according to the invention the film coat enveloping 10 the core of the tablet according to the invention comprises hydroxypropyl methylcellulose, polyethyleneglycol, titanium dioxide, talc and iron oxides, preferably iron oxide red. <br><br>
The pharmaceutical composition according to the invention can be prepared 15 according to the procedure outlined in detail in the experimental section of this patent application. <br><br>
In the light of the pharmaceutical efficacy of flibanserin, the present invention furthermore relates to the use of the flibanserin polymorph A containing formulations 20 according to the invention as a medicament. <br><br>
A further aspect of the present invention relates to the use of the flibanserin polymorph A containing formulations according to the invention for treating diseases in which the use of compounds displaying affinity for the 5-HTia and 5-HT2-receptor may have a therapeutic benefit. <br><br>
A further aspect of the present invention relates to the use of the flibanserin polymorph A containing formulations according to the invention for treating a disease selected from depression, schizophrenia, Parkinson, anxiety, sleep disturbances, 30 sexual and mental disorders and age associated memory impairment. <br><br>
In particular, the instant invention relates to the use of the flibanserin polymorph A containing formulations according to the invention for the treatment of disorders of sexual desire. <br><br>
35 <br><br>
In a preferred embodiment the invention relates to the use of the flibanserin polymorph A containing formulations according to the invention for the treatment of disorders selected from the group consisting of Hypoactive Sexual Desire Disorder, <br><br>
WO 03/097058 PCT/EP03/05226 <br><br>
8 <br><br>
loss of sexual desire, lack of sexual desire, decreased sexual desire, inhibited sexual desire, loss of libido, libido disturbance, and frigidity. <br><br>
Particular preferred according to the invention is the use of the flibanserin polymorph 5 A containing formulations according to the invention for the treatment of disorders selected from the group consiting of Hypoactive Sexual Desire Disorder, loss of sexual desire, lack of sexual desire, decreased sexual desire, inhibited sexual desire. In a particularily preferred embodiment the invention relates to the use of the flibanserin polymorph A containing formulations according to the invention for the 10 treatment of disorders selected from the group of Hypoactive Sexual Desire Disorder and loss of sexual desire. <br><br>
Another aspect of the present invention relates to a method for treating diseases in which the use of compounds displaying affinity for the 5-HT-ia and 5-HT2-receptor 15 may have a therapeutic benefit comprising the administration of a flibanserin polymorph A containing formulations according to the invention. <br><br>
A further aspect of the present invention relates to a method for treating a disease selected from depression, schizophrenia, Parkinson, anxiety, sleep disturbances, 20 sexual and mental disorders and age associated memory impairment comprising the administration of a flibanserin polymorph A containing formulations according to the invention. <br><br>
In particular, the instant invention relates to a method for the treatment of disorders 0J)25 of sexual desire comprising the administration of a flibanserin polymorph A containing formulations according to the invention. <br><br>
In a preferred embodiment the invention relates to a method for the treatment of disorders selected from the group consisting of Hypoactive Sexual Desire Disorder, 30 loss of sexual desire, lack of sexual desire, decreased sexual desire, inhibited sexual desire, loss of libido, libido disturbance, and frigidity, comprising the administration of a flibanserin polymorph A containing formulations according to the invention. <br><br>
Particular preferred according to the invention is a method for the treatment of 35 disorders selected from the group consiting of Hypoactive Sexual Desire Disorder, loss of sexual desire, lack of sexual desire, decreased sexual desire, inhibited sexual desire comprising the administration of a flibanserin polymorph A containing formulations according to the invention. <br><br>
WO 03/097058 PCT/EP03/05226 <br><br>
9 <br><br>
In a particularity preferred embodiment the invention relates to a method for the treatment of disorders selected from the group of Hypoactive Sexual Desire Disorder and loss of sexual desire, comprising the administration of a flibanserin polymorph A containing formulations according to the invention. <br><br>
5 <br><br>
The aforementioned therapeutic effects of the flibanserin polymorph A containing formulations according to the invention can be achieved in men and women. However, according to a further aspect of the invention the use of the flibanserin polymorph A containing formulations according to the invention for the treatment of 10 female sexual dysfunction is preferred. <br><br>
4^0 The beneficial effects of the flibanserin polymorph A containing formulations according to the invention can be observed regardless of whether the disturbance existed lifelong or was acquired, and independent of etiologic origin (organic - both, 15 physically and drug induced-, psychogen, a combination of organic - both, physically and drug induced-, and psychogen, or unknown). <br><br>
The invention will be further described by the following examples. These examples disclose certain preferred embodiments of the invention. Accordingly, it is intended 20 that the invention be not limited to the following explicitly disclosed examples. <br><br>
Synthesis of flibanserin polymorph A: <br><br>
375 kg of 1-[(3-trif!uoromethyl)phenyl]-4-(2-cloroethyl)piperazin are charged in a reactor with-2500 kg of water and 200 kg of aqueous Sodium Hydroxide 45%. Under stirring 169.2 kg of 1-(2-propenyl)-1,3-dihydro-benzimidazol-2H-one, 780 kg of isopropanol, 2000 kg of water and 220 kg of aqueous Sodium Hydroxide 45% are added. The reaction mixture is heated to 75-85°C and 160 kg of concentrated hydrochloric acid and 200 kg of water are added. The reaction mixture is stirred at constant temperature for about 45 minutes. After distillation of a mixture of water and Isopropanol (about 3000 kg) the remaining residue is cooled to about 65-75°C and the pH is adjusted to 6.5 - 7.5 by addition of 125 kg of aqueous Sodium Hydroxide 45%. After cooling to a temperature of 45-50°C, the pH value is adjusted to 8-9 by addition of about 4 kg of aqueous Sodium Hydroxide 45%.Subsequently the mixture is cooled to 30-35°C and centrifuged. The residue thus obtained is washed with 3401 of water and 1261 of isopropanol and then with water until chlorides elimination. The wet product is dried under vacuum at a temperature of about 45-55°C which leads to 358 kg of crude flibanserin polymorph A. The crude product thus obtained is loaded in a reactor with 1750 kg of Acetone and the resulting mixture is heated under stirring until reflux. The obtained solution is filtered and the filtrate is concentrated by <br><br>
WO 03/097058 <br><br>
PCT/EP03/05226 <br><br>
10 <br><br>
distillation. The temperature is maintained for about 1 hour 0-5°C, then the precipitate solid is isolated by filtration and dried at 55°C for at least 12 hours. The final yield is 280 kg of pure flibanserin polymorph A. <br><br>
5 Characterisation of flibanserin polymorph A: <br><br>
Flibanserin polymorph A was characterised by DSC (Differantial Scanning Calorimetry). The peak temperature determined for polymorph A is about 161 °C. For the characterization via DSC a Mettler TA 3000 System equipped with TC 10-A processor and DSC 20 cell was applied. The heating rate was 10 K/min. <br><br>
10 <br><br>
The flibanserin polymorph A was additionally characterised by powder x-ray diffractometry. The x-ray powder diffraction pattern for polymorph A was obtained according to the following conditions: <br><br>
15 Equipment: Philips PW 1800/10 diffractometer equipped with a digital microvax 2000. <br><br>
20 <br><br>
Setting parameters: X-rav <br><br>
Type tube: Wavelenghts (X): <br><br>
Koti =1.54060 A Ko2 = 1-54439 A 0.500 <br><br>
Cu (long fine focus) <br><br>
Intensity ratio (a2/ a1): <br><br>
* <br><br>
>5 <br><br>
Start angle [°2©]: End angle [°2©]: Step size [°2©]: <br><br>
2.000 <br><br>
60.000 <br><br>
0.020 <br><br>
Maximum intensity[sj: <br><br>
7310.250 <br><br>
Type of scan: <br><br>
continuous <br><br>
30 <br><br>
35 <br><br>
Minimum peak tip width: 0.00 <br><br>
Maximum peak tip width: 1.00 <br><br>
Peak base width: 2.00 <br><br>
Minimum significance: 0.75 <br><br>
Number of peaks: 69 <br><br>
Generator: <br><br>
high voltage: <br><br>
tube current: <br><br>
50 KV 30 mA <br><br>
WO 03/097058 PCT/EP03/05226 <br><br>
11 <br><br>
The powder x-ray diffraction pattern obtained for polymorph A is illustrated in figure 1. The appropiate values are collected in table 1. <br><br>
Table 1: <br><br>
Angle d-value d-value <br><br>
Peak width <br><br>
Peak int <br><br>
Back, int <br><br>
Rel. int <br><br>
Signif. <br><br>
P201 <br><br>
oci rAi oc 2 [Al r°20l <br><br>
(counts! <br><br>
[counts] <br><br>
[%] <br><br>
5.195 <br><br>
16.9967 <br><br>
17.0390 <br><br>
0.960 <br><br>
8 <br><br>
69 <br><br>
0.1 <br><br>
1.05 <br><br>
9.045 <br><br>
9.7689 <br><br>
9.7931 <br><br>
0.100 <br><br>
92 <br><br>
96 <br><br>
1.3 <br><br>
0.97 <br><br>
9.335 <br><br>
9.4660 <br><br>
9.4896 <br><br>
0.080 <br><br>
114 <br><br>
98 <br><br>
1.6 <br><br>
0.88 <br><br>
10.025 <br><br>
8.8160 <br><br>
8.8379 <br><br>
0.140 <br><br>
400 <br><br>
100 <br><br>
5.5 <br><br>
7.18 <br><br>
10.595 <br><br>
8.3430 <br><br>
8.3637 <br><br>
0.140 <br><br>
204 <br><br>
102 <br><br>
2.8 <br><br>
3.46 <br><br>
11.290 <br><br>
7.8309 <br><br>
7.8503 <br><br>
0.140 <br><br>
467 <br><br>
104 <br><br>
6.4 <br><br>
6.91 <br><br>
13.225 <br><br>
6.6891 <br><br>
6.7058 <br><br>
0.180 <br><br>
548 <br><br>
112 <br><br>
7.5 <br><br>
13.10 <br><br>
14.595 <br><br>
6.0642 <br><br>
6.0793 <br><br>
0.180 <br><br>
404 <br><br>
121 <br><br>
5.5 <br><br>
9.17 <br><br>
15.460 <br><br>
5.7268 <br><br>
5.7410 <br><br>
0,140 <br><br>
4186 <br><br>
125 <br><br>
57.3 <br><br>
23.20 <br><br>
16.655 <br><br>
5.3185 <br><br>
5.3317 <br><br>
0.200 <br><br>
515 <br><br>
130 <br><br>
7.0 <br><br>
12.38 <br><br>
17.085 <br><br>
5.1856 <br><br>
5.1985 <br><br>
0.100 <br><br>
1347 <br><br>
132 <br><br>
18.4 <br><br>
2.78 <br><br>
17.285 <br><br>
5.1260 <br><br>
5.1388 <br><br>
0.060 <br><br>
1399 <br><br>
135 <br><br>
19.1 <br><br>
2.26 <br><br>
17.420 <br><br>
5.0866 <br><br>
5.0992 <br><br>
0.100 <br><br>
1204 <br><br>
135 <br><br>
16.5 <br><br>
4.71 <br><br>
18.140 <br><br>
4.8863 <br><br>
4.8984 <br><br>
0.180 <br><br>
1043 <br><br>
139 <br><br>
14.3 <br><br>
13.14 <br><br>
18.650 <br><br>
4.7538 <br><br>
4.7656 <br><br>
0.120 <br><br>
1063 <br><br>
142 <br><br>
14.5 <br><br>
0.91 <br><br>
19.140 <br><br>
4.6332 <br><br>
4.6447 <br><br>
0.140 <br><br>
7310 <br><br>
144 <br><br>
100.0 <br><br>
32.77 <br><br>
19.820 <br><br>
4.4757 <br><br>
4.4869 <br><br>
0.160 <br><br>
3624 <br><br>
146 <br><br>
49.6 <br><br>
9.02 <br><br>
20.080 <br><br>
4.4184 <br><br>
4.4294 <br><br>
0.140 <br><br>
5402 <br><br>
149 <br><br>
73.9 <br><br>
21.06 <br><br>
20.385 <br><br>
4.3530 <br><br>
4.3638 <br><br>
0.160 <br><br>
2652 <br><br>
149 <br><br>
36.3 <br><br>
23.25 <br><br>
21.215 <br><br>
4.1845 <br><br>
4.1949 <br><br>
0.160 <br><br>
369 <br><br>
154 <br><br>
5.0 <br><br>
5.78 <br><br>
21.890 <br><br>
4.0570 <br><br>
4.0670 <br><br>
0.200 <br><br>
773 <br><br>
156 <br><br>
10.6 <br><br>
3.09 <br><br>
22.630 <br><br>
3.9259 <br><br>
3.9357 <br><br>
0.280 <br><br>
4277 <br><br>
161 <br><br>
58.5 <br><br>
74.66 <br><br>
23.210 <br><br>
3.8291 <br><br>
3.8386 <br><br>
0.120 <br><br>
484 <br><br>
164 <br><br>
6.6 <br><br>
3.33 <br><br>
24.355 <br><br>
3.6516 <br><br>
3.6607 <br><br>
0.060 <br><br>
2725 <br><br>
169 <br><br>
37.3 <br><br>
1.16 <br><br>
24.610 <br><br>
3.6144 <br><br>
3.6234 <br><br>
0.140 <br><br>
3540 <br><br>
172 <br><br>
48.4 <br><br>
17.08 <br><br>
24.995 <br><br>
3.5596 <br><br>
3.5684 <br><br>
0.100 <br><br>
529 <br><br>
174 <br><br>
7.2 <br><br>
1.01 <br><br>
25.260 <br><br>
3.5228 <br><br>
3.5316 <br><br>
0.120 <br><br>
557 <br><br>
174 <br><br>
7.6 <br><br>
3.02 <br><br>
26.575 <br><br>
3.3514 <br><br>
3.3597 <br><br>
0.240 <br><br>
2421 <br><br>
182 <br><br>
33.1 <br><br>
42.58 <br><br>
27.155 <br><br>
3.2811 <br><br>
3.2893 <br><br>
0.140 <br><br>
676 <br><br>
185 <br><br>
9.2 <br><br>
1.32 <br><br>
27.310 <br><br>
3.2629 <br><br>
3.2710 <br><br>
0.100 <br><br>
767 <br><br>
185 <br><br>
10.5 <br><br>
2.75 <br><br>
27.865 <br><br>
3.1991 <br><br>
3.2071 <br><br>
0.120 <br><br>
420 <br><br>
188 <br><br>
5.7 <br><br>
1.08 <br><br>
28.210 <br><br>
3.1608 <br><br>
3.1686 <br><br>
0.100 <br><br>
1467 <br><br>
190 <br><br>
20.1 <br><br>
0.79 <br><br>
WO 03/097058 PCT/EP03/05226 <br><br>
12 <br><br>
Table 1 (continued): <br><br>
Angle d-value d-value <br><br>
Peak width <br><br>
Peak int <br><br>
Back, int <br><br>
Rel. int <br><br>
Signif. <br><br>
r°201 <br><br>
cc1[A] <br><br>
a2 rAl r°201 <br><br>
[counts] <br><br>
[counts! <br><br>
[%1 <br><br>
28.325 <br><br>
3.1482 <br><br>
3.1560 <br><br>
0.140 <br><br>
1789 <br><br>
190 <br><br>
24.5 <br><br>
4.41 <br><br>
28.650 <br><br>
3.1132 <br><br>
3.1210 <br><br>
0.180 <br><br>
1204 <br><br>
190 <br><br>
16.5 <br><br>
11.65 <br><br>
29.520 <br><br>
3.0234 <br><br>
3.0309 <br><br>
0.220 <br><br>
1011 <br><br>
196 <br><br>
13.8 <br><br>
15.74 <br><br>
30.250 <br><br>
2.9521 <br><br>
2.9594 <br><br>
0.120 <br><br>
159 <br><br>
199 <br><br>
2.2 <br><br>
1.22 <br><br>
31.105 <br><br>
2.8729 <br><br>
2.8800 <br><br>
0.360 <br><br>
282 <br><br>
204 <br><br>
3.9 <br><br>
8.14 <br><br>
31.905 <br><br>
2.8026 <br><br>
2.8096 <br><br>
0.100 <br><br>
339 <br><br>
207 <br><br>
4.6 <br><br>
0.96 <br><br>
32.350 <br><br>
2.7651 <br><br>
2.7720 <br><br>
0.120 <br><br>
237 <br><br>
210 <br><br>
3.2 <br><br>
3.01 <br><br>
33.300 <br><br>
2.6884 <br><br>
2.6950 <br><br>
0.180 <br><br>
1347 <br><br>
216 <br><br>
18.4 <br><br>
14.06 <br><br>
33.640 <br><br>
2.6620 <br><br>
2.6686 <br><br>
0.100 <br><br>
404 <br><br>
216 <br><br>
5.5 <br><br>
1.45 <br><br>
34.880 <br><br>
2.5701 <br><br>
2.5765 <br><br>
0.200 <br><br>
202 <br><br>
222 <br><br>
2.8 <br><br>
1.04 <br><br>
35.275 <br><br>
2.5422 <br><br>
2.5486 <br><br>
0.240 <br><br>
299 <br><br>
225 <br><br>
4.1 <br><br>
4.84 <br><br>
36.055 <br><br>
2.4890 <br><br>
2.4952 <br><br>
0.280 <br><br>
202 <br><br>
228 <br><br>
2.8 <br><br>
3.78 <br><br>
36.910 <br><br>
2.4333 <br><br>
2.4393 <br><br>
0.320 <br><br>
169 <br><br>
234 <br><br>
2.3 <br><br>
0.90 <br><br>
37.160 <br><br>
2.4175 <br><br>
2.4235 <br><br>
0.120 <br><br>
216 <br><br>
234 <br><br>
3.0 <br><br>
2.14 <br><br>
37.680 <br><br>
2.3853 <br><br>
2.3912 <br><br>
0.240 <br><br>
240 <br><br>
237 <br><br>
3.3 <br><br>
1.58 <br><br>
39.435 <br><br>
2.2831 <br><br>
2.2888 <br><br>
0.280 <br><br>
449 <br><br>
246 <br><br>
6.1 <br><br>
2.67 <br><br>
39.675 <br><br>
2.2698 <br><br>
2.2755 <br><br>
0.080 <br><br>
396 <br><br>
246 <br><br>
5.4 <br><br>
0.82 <br><br>
40.325 <br><br>
2.2347 <br><br>
2.2403 <br><br>
0.160 <br><br>
520 <br><br>
250 <br><br>
7.1 <br><br>
0.95 <br><br>
40.930 <br><br>
2.2031 <br><br>
2.2086 <br><br>
0.120 <br><br>
480 <br><br>
253 <br><br>
6.6 <br><br>
2.66 <br><br>
41.445 <br><br>
2.1769 <br><br>
2.1823 <br><br>
0.240 <br><br>
372 <br><br>
256 <br><br>
5.1 <br><br>
2.65 <br><br>
41.990 <br><br>
2.1499 <br><br>
2.1552 <br><br>
0.120 <br><br>
538 <br><br>
259 <br><br>
7.4 <br><br>
1.31 <br><br>
42.670 <br><br>
2.1172 <br><br>
2.1225 <br><br>
0.160 <br><br>
428 <br><br>
262 <br><br>
5.9 <br><br>
1.45 <br><br>
43.145 <br><br>
2.0950 <br><br>
2.1002 <br><br>
0.120 <br><br>
433 <br><br>
266 <br><br>
5.9 <br><br>
1.50 <br><br>
44.190 <br><br>
2.0478 <br><br>
2.0529 <br><br>
0.160 <br><br>
376 <br><br>
269 <br><br>
5.1 <br><br>
0.89 <br><br>
46.095 <br><br>
1.9675 <br><br>
1.9724 <br><br>
0.160 <br><br>
279 <br><br>
279 <br><br>
3.8 <br><br>
0.86 <br><br>
46.510 <br><br>
1.9509 <br><br>
1.9558 <br><br>
0.240 <br><br>
310 <br><br>
282 <br><br>
4.2 <br><br>
0.87 <br><br>
48.305 <br><br>
1.8826 <br><br>
1.8872 <br><br>
0.200 <br><br>
506 <br><br>
292 <br><br>
6.9 <br><br>
2.06 <br><br>
48.900 <br><br>
1.8610 <br><br>
1.8657 <br><br>
0.240 <br><br>
615 <br><br>
296 <br><br>
8.4 <br><br>
1.67 <br><br>
50.330 <br><br>
1.8115 <br><br>
1.8160 <br><br>
0.160 <br><br>
437 <br><br>
.303 <br><br>
6.0 <br><br>
1.73 <br><br>
51.035 <br><br>
1.7881 <br><br>
1.7925 <br><br>
0.080 <br><br>
416 <br><br>
306 <br><br>
5.7 <br><br>
0.93 <br><br>
53.550 <br><br>
1.7099 <br><br>
1.7141 <br><br>
0.480 <br><br>
177 <br><br>
317 <br><br>
2.4 <br><br>
2.84 <br><br>
54.500 <br><br>
1.6823 <br><br>
1.6865 <br><br>
0.400 <br><br>
130 <br><br>
324 <br><br>
1.8 <br><br>
1.37 <br><br>
55.420 <br><br>
1.6565 <br><br>
1.6606 <br><br>
0.320 <br><br>
130 <br><br>
328 <br><br>
1.8 <br><br>
1.72 <br><br>
56.220 <br><br>
1.6348 <br><br>
1.6389 <br><br>
0.320 <br><br>
121 <br><br>
331 <br><br>
1.7 <br><br>
0.87 <br><br>
56.770 <br><br>
1.6203 <br><br>
1.6243 <br><br>
0.240 <br><br>
142 <br><br>
335 <br><br>
1.9 <br><br>
1.59 <br><br>
WO 03/097058 <br><br>
Table 1 (continued): <br><br>
13 <br><br>
PCT/EP03/05226 <br><br>
Angle d-value d-value Peak width Peak int Back, int Rel. int Signif. <br><br>
f°201 a1 rAl a 2 fA] [°201 [counts] [counts] [%] <br><br>
57.405 1.6039 1.6079 0.240 112 339 1.5 1.19 <br><br>
58.500 1.5764 1.5804 0.240 67 342 0.9 1.57 <br><br>
Manufacturing of flibanserin containing film-coated tablets: <br><br>
A) Equipment used: <br><br>
The following equipment was used in the method of preparation of the pharmaceutical composition according to the invention: <br><br>
Mixing vessel with Ekato stirrer and Ultra Turrax for granulation liquid and film 10 coating suspension; <br><br>
high shear mixer/granulator (e.g. Diosna P 400); <br><br>
wet screen machine (e.g. Alexanderwerk); <br><br>
fluid bed dryer (e.g. Glatt WSG 15); <br><br>
dry screen machine (e.g. Quadro Comil AS 197); <br><br>
15 free fall blender (e.g. Servolift 120 I or container mixer); <br><br>
rotary tablet press (e.g. Fette P 1200); <br><br>
film coater (e.g. Glatt GC1250); <br><br>
B) Process description: <br><br>
20 As a first step the granulation liquid for the wet granulation process ist prepared. Purified water is filled into a suitable mixing vessel and heated to about 80°C. Then Hypromeliose (Methocel E5 Prem) and/or additional wet binding components are stirred in, and the dispersion is cooled down to room temperature. If necessary, the liquid is allowed to stand overnight (completeness of solution / reduction of frothing) 25 and stirred up before use. If necessary, any weight loss is compensated with purified water. The dry matter (soldis content) of this granulation liquid is preferrably in the range of 4-6%. <br><br>
For the granulation process Lactose monohydrate, fine milled and sieved, the 30 required quantity of Flibanserin polymorph A (depending on the dose strength), micronized quality, and Cellulose, microcrystalline (Avicel PH 101) are filled in in this order, mixed homogeneously for about 4 minutes using impeller and chopper blades. Next the granulation liquid is added either manually or by spray nozzles and the wet mass is granulated for about 2-3 minutes, again using impeller and chopper blades. 35 After discharging of the high shear mixer/granulator the wet granules are wet- <br><br>
WO 03/097058 <br><br>
PCT/EP03/05226 <br><br>
14 <br><br>
screened through a 3.0 mm mesh size sieve to destroy large agglomerates. The wet-screened material is transferred to a conventional fluid bed drier (or alternatively to a tray drier) and dried at an inlet air temperature of approximately 100 °C until an exhaust air temperature (or alternatively product temperature) of approximately 50°C 5 (45-55°C) is reached. The residual moisture of the granulate in terms of loss on drying should be in the range of 0.5-1.5 %. The dried granules are then dry screened with the help of a Comil screen machine using a 2 mm rasp screen. Finally, the screened granulate is filled into a suitable free-fall blender, e.g. a container mixer, the crosslinked Carboxymethylcellulose sodium (Croscarmellose sodium, brand 10 name: Ac-Di-Sol) and Magnesium stearate are added, and the components are mixed for 10-20 minutes, preferrably 15 minutes, at a mixing speed of 10 rpm until homogeneous. <br><br>
The final tableting mixture is compressed on a suitable tablets press (e.g. rotary press) to the respective target weight of the required dose strength of Flibanserin 15 tablets using the appropriate tools (e.g. in case of 50 mg tablets: 9 mm round, biconvex, with bevelled edges; or in case of 100 mg tablets: 14x6.8 mm oblong shaped). Predetermined hardness specifications for the different tool dimensions have to be followed in order to achieve the intended drug dissolution profile and product characteristics. <br><br>
20 Since the drug substance Flibanserin is of bitter taste and slightly light sensitive, a protecting film coat has to be applied to the tablet cores in order to achieve a stable and consumer friendly product. To this end a coating suspension is prepared by filling purified water into a suitable mixing vessel, and dissolving polyethyleneglycol . 6000 and then hydroxypropylmethylcellulose with the help of a high intensity stirrer. <br><br>
^£^25 In a next step an aqueous slurry of titanium dioxide, talc and iron oxide red (in case of coloured film tablets) is poured and stirred into the film-forming polymer solution. The dry matter of this coating suspension is in the range of 10-15 %, preferrably about 12-13%. <br><br>
The above prepared tablet cores are filled into a suitable film coater (e.g. an Accela 30 Cota with a 36" pan, or a Glatt GC 1250 Coater with perforated pan, and top spray system), and preheated up to a temperature of approximately 50 °C. After this product temperature is reached the coating suspension is sprayed onto the cores with the help of one or more spray nozzles at a spray pressure of about 2 bar, a spray rate of about 4 kg/h (in case of Accela Cota), an inlet air temperature of about 35 60-85°C. it is important to control and maintain the product temperature during spraying at a level of between 48-52° C to achieve a high quality film-coat. After the spraying is finished the film-coated tablets are cooled down to approx. 30°C before the equipment is discharged. The total process time for the film-coating is in the range of 2-3 hours. <br><br>
WO 03/097058 <br><br>
PCT/EP03/05226 <br><br>
15- <br><br>
After all in-process and quality controls have been performed the bulk film-coated tablets are now ready for primary packaging into the respective marketing presentations (e.g. PVC/PVDC blister packs or HDPE bottles). <br><br>
5 The following film-coated tablets were obtained in analogy to the method of preparation described hereinbefore. <br><br>
Example N°1 - Composition <br><br>
Core <br><br>
Constituents mg/tablet <br><br>
Flibanserin polymorph A <br><br>
25.000 <br><br>
Lactose monohydrate <br><br>
71.720 <br><br>
Microcrystalline cellulose <br><br>
23.905 <br><br>
HPMC (Methocel E5) <br><br>
1.250 <br><br>
Carboxymethylcellulose sodium <br><br>
2.500 <br><br>
Magnesium stearate <br><br>
0.625 <br><br>
10 <br><br>
Coating <br><br>
Constituents mg/tablet <br><br>
HPMC (Methocel E5) <br><br>
1.440 <br><br>
Polyethylene Glycol 6000 <br><br>
0.420 <br><br>
Titanium dioxide <br><br>
0.600 <br><br>
Talc <br><br>
0.514 <br><br>
Iron oxide red <br><br>
0.026 <br><br>
Total Film coated tablet <br><br>
128.000 <br><br>
WO 03/097058 PCT/EP03/05226 <br><br>
16 <br><br>
Example N°2 - Composition <br><br>
Core <br><br>
Constituents mg/tablet <br><br>
Flibanserin polymorph A <br><br>
50.000 <br><br>
Lactose monohydrate <br><br>
143.440 <br><br>
Microcrystalline cellulose <br><br>
47.810 <br><br>
HPMC (e.g. Pharmacoat 606) <br><br>
2.500 <br><br>
Carboxymethylcellulose sodium <br><br>
5.000 <br><br>
Magnesium stearate <br><br>
1.250 <br><br>
Coating <br><br>
Constituents mg/ tablet <br><br>
HPMC (e.g. Pharmacoat 606) <br><br>
2.400 <br><br>
Polyethylene Glycol 6000 <br><br>
0.700 <br><br>
Titanium dioxide <br><br>
1.000 <br><br>
Talc <br><br>
0.857 <br><br>
Iron oxide red <br><br>
0.043 <br><br>
Total Film coated tablet <br><br>
255.000 <br><br>
Example N°3 - Composition Core <br><br>
Constituents mg/tablet <br><br>
Flibanserin polymorph A <br><br>
100.000 <br><br>
Lactose monohydrate <br><br>
171.080 <br><br>
Microcrystalline cellulose <br><br>
57.020 <br><br>
HPMC (e.g. Methocel E5) <br><br>
3.400 <br><br>
Carboxymethylcellulose sodium <br><br>
6.800 <br><br>
Magnesium stearate <br><br>
1.700 <br><br>
WO 03/097058 <br><br>
PCT/EP03/05226 <br><br>
17 <br><br>
Coating <br><br>
Constituents mg/ tablet <br><br>
HPMC (e.g. Methocel E5) <br><br>
3.360 <br><br>
Polyethylene Glycol 6000 <br><br>
0.980 <br><br>
Titanium dioxide <br><br>
1.400 <br><br>
Talc <br><br>
1.200 <br><br>
Iron oxide red <br><br>
0.060 <br><br>
Total Film coated tablet <br><br>
347.000 <br><br>
Example N°4 - Composition <br><br>
Core <br><br>
Constituents mg/tablet <br><br>
Flibanserin polymorph A <br><br>
2.000 <br><br>
Dibasic Calciumphosphate, anhydrous <br><br>
61.010 <br><br>
Microcrystalline cellulose <br><br>
61.010 <br><br>
HPMC (Methocel E5) <br><br>
1.950 <br><br>
Carboxymethylcellulose sodium <br><br>
2.600 <br><br>
Colloidal silicon dioxide <br><br>
0.650 <br><br>
Magnesium stearate <br><br>
0.780 <br><br>
Coating <br><br>
Constituents mg/ tablet <br><br>
HPMC (Methocel E5) <br><br>
1.440 <br><br>
Polyethylene Glycol 6000 <br><br>
0.420 <br><br>
Titanium dioxide <br><br>
0.600 <br><br>
Talc <br><br>
0.514 <br><br>
Iron oxide red <br><br>
0.026 <br><br>
Total Film coated tablet <br><br>
133.000 <br><br>
WO 03/097058 PCT/EP03/05226 <br><br>
18 <br><br>
Example N°5 - Composition <br><br>
Core <br><br>
Constituents mg/tablet <br><br>
Flibanserin polymorph A <br><br>
100.000 <br><br>
Dibasic Calciumphosphate, anhydrous <br><br>
69.750 <br><br>
Microcrystalline cellulose <br><br>
69.750 <br><br>
HPMC (e.g. Methocel E5) <br><br>
2.750 <br><br>
Carboxymethylcellulose sodium <br><br>
5.000 <br><br>
Colloidal silicon dioxide <br><br>
1.250 <br><br>
Magnesium stearate <br><br>
1.500 <br><br>
5 Coating <br><br>
Constituents mg/ tablet <br><br>
HPMC (e.g. Methocel E5) <br><br>
2.400 <br><br>
Polyethylene Glycol 6000 <br><br>
0.700 <br><br>
Titanium dioxide <br><br>
1.043 <br><br>
Talc <br><br>
0.857 <br><br>
Total Film coated tablet <br><br>
255.000 <br><br>
10 <br><br>
Example N°6 - Composition <br><br>
Core <br><br>
Constituents mg/tablet <br><br>
Flibanserin polymorph A <br><br>
20.000 <br><br>
Lactose monohydrate <br><br>
130.000 <br><br>
Microcrystalline cellulose <br><br>
43.100 <br><br>
Hydroxypropyl Cellulose (e.g. Klucel LF) <br><br>
1.900 <br><br>
Sodium Starch Glycolate <br><br>
4.000 <br><br>
Magnesium.stearate <br><br>
1.000 <br><br></p>
</div>